Job Description

**General Description:** We are seeking a highly skilled and dedicated Statistician with a specialized focus on Patient Reported Outcome (PRO) analyses to join our dynamic team. The ideal candidate will have a strong background in statistical methodologies and experience in handling patient-reported data to draw meaningful insights. Functioning as a mentor or manager in the stat group. Located in EU or US. **Essential Functions of the job:** This role is crucial in advancing our understanding of patient experiences and improving healthcare outcomes through rigorous analytical approaches. **Responsibilities:** + Data Management and Analysis: Conduct statistical analyses on patient-reported outcome data, ensuring accuracy, validity, and reliability of results. + Methodological Development: Develop and implement advanced statistical methods and models tailored to patient-reported outcome measures (PROMs). + Research and Reporting: Lead research projects involving PRO analyses, prepare comprehensive reports, and present findings to stakeholders. + Collaboration: Work closely with cross-functional teams, including clinical researchers, data scientists, and healthcare professionals, to integrate PRO data into broader research initiatives. + Data Interpretation: Translate complex statistical findings into actionable insights that can inform clinical practices and policy decisions. + Quality Assurance: Ensure the highest standards of data quality and integrity in all analyses and reports. + Training and Mentorship: Provide guidance and support to junior statisticians and other team members in the area of PRO analyses. **Computer Skills:** Microsoft office apps, SAS and R **Other Qualifications:** + PhD or equivalent degree in statistics/biostatistics or related discipline with a minimum of 5 years relevant work experience, or a Master's degree with a minimum of 7 years relevant work experience (see each box for detailed year requirement). + Experience in the healthcare or pharmaceutical industry. + Familiarity with regulatory guidelines related to patient-reported outcomes. + Published research in peer-reviewed journals on topics related to PRO analyses. + Experience in designing and validating patient-reported outcome measures. + Solid knowledge of statistical analysis methodologies and experimental design. + Solid working knowledge of statistical and data processing software e.g. SAS and/or R. + Strong good presentation, oral and written communication skills. + Ability to learn, being proactive, motivated, and consistently focus on details and execution. + Strong demonstrates interest in statistical research activities and application of novel methods to clinical trial development. + Ability to work in a team environment with clinical team members. + Knowledge of clinical trial design concepts; In-depth knowledge of all phases of the drug development process. + Demonstrated skill in the planning, analysis and reporting of clinical trials. **Travel:** Yes, depends on needs. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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